Walbaum R, François P, Farriaux J P, Woillez M
Hum Genet. 1978 Oct 31;44(2):219-26. doi: 10.1007/BF00295418.
A partial monosomy 13 by interstitial deletion was found in the complement of a girl with mild mental retardation and bilateral retinoblastoma. Break points were at 13q12 and 13q14. After comparison with other known observations of retinoblastoma with deletion of chromosome 13, it is suggested that the deletion common to these patients may be band 13q14. The most likely pathogenic hypothesis seems to be the haplo-insufficiency.
在一名患有轻度智力障碍和双侧视网膜母细胞瘤的女孩的染色体组中发现了因中间缺失导致的13号染色体部分单体性。断点位于13q12和13q14。在与其他已知的13号染色体缺失的视网膜母细胞瘤观察结果进行比较后,提示这些患者共有的缺失可能是13q14带。最可能的致病假说似乎是单倍体不足。